Literature DB >> 21834028

Physical health problems in adults with Prader-Willi syndrome.

Margje Sinnema1, Marian A Maaskant, Henny M J van Schrojenstein Lantman-de Valk, I Caroline van Nieuwpoort, Madeleine L Drent, Leopold M G Curfs, Constance T R M Schrander-Stumpel.   

Abstract

Prader-Willi syndrome (PWS) is a genetic disorder which is characterized by severe hypotonia and feeding problems in early infancy. In later childhood and adolescence, this is followed by hyperphagia and extreme obesity if the diet is not strictly controlled. Data on physical health problems in adults with PWS are scarce. We report on the prevalence of physical health problems in a Dutch cohort of adults with PWS in relation to age, BMI, and genetic subtype. Participants (n = 102) were retrieved via the Dutch Prader-Willi Parent Association and through physicians specializing in persons with intellectual disabilities (ID). Details regarding physical health problem spanning the participants' lifespan were collected from caretakers through semi-structured interviews. Cardiovascular problems included diabetes mellitus, hypertension, and cerebrovascular accidents. Respiratory infections were frequent in adulthood. In males, cryptorchidism was almost universal, for which 28/48 males had a history of surgery, mostly orchidopexy. None of the women had a regular menstrual cycle. Sixteen individuals had a diagnosis of osteoporosis. Spinal deformation, hip dysplasia, and foot abnormalities were common. Skinpicking, leg edema, and erysipelas were frequent dermatological problems. The findings in our group support the notion that the prevalence of physical health problems is underestimated. This underscores the importance of developing monitoring programs which would help to recognize physical health problems at an early stage.
Copyright © 2011 Wiley-Liss, Inc.

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Year:  2011        PMID: 21834028     DOI: 10.1002/ajmg.a.34171

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  22 in total

1.  Contributing factors of mortality in Prader-Willi syndrome.

Authors:  Jennifer Proffitt; Kathryn Osann; Barbara McManus; Virginia E Kimonis; Janalee Heinemann; Merlin G Butler; David A Stevenson; June-Anne Gold
Journal:  Am J Med Genet A       Date:  2018-12-19       Impact factor: 2.802

Review 2.  Update on Diabetes Mellitus and Glucose Metabolism Alterations in Prader-Willi Syndrome.

Authors:  Antonino Crinò; Graziano Grugni
Journal:  Curr Diab Rep       Date:  2020-02-06       Impact factor: 4.810

3.  Long-term outcome of epilepsy in patients with Prader-Willi syndrome.

Authors:  Alberto Verrotti; Raffaella Cusmai; Daniela Laino; Marco Carotenuto; Maria Esposito; Raffaele Falsaperla; Lucia Margari; Renata Rizzo; Salvatore Savasta; Salvatore Grosso; Pasquale Striano; Vincenzo Belcastro; Emilio Franzoni; Paolo Curatolo; Lucio Giordano; Elena Freri; Sara Matricardi; Dario Pruna; Irene Toldo; Elisabetta Tozzi; Lucio Lobefalo; Francesca Operto; Emma Altobelli; Francesco Chiarelli; Alberto Spalice
Journal:  J Neurol       Date:  2014-10-18       Impact factor: 4.849

Review 4.  Recommendations for the diagnosis and management of childhood Prader-Willi syndrome in China.

Authors:  Dai Yang-Li; Luo Fei-Hong; Zhang Hui-Wen; Ma Ming-Sheng; Luo Xiao-Ping; Liu Li; Wang Yi; Zhou Qing; Jiang Yong-Hui; Zou Chao-Chun
Journal:  Orphanet J Rare Dis       Date:  2022-06-13       Impact factor: 4.303

5.  Disruption of MBD5 contributes to a spectrum of psychopathology and neurodevelopmental abnormalities.

Authors:  J C Hodge; E Mitchell; V Pillalamarri; T L Toler; F Bartel; H M Kearney; Y S Zou; W H Tan; C Hanscom; S Kirmani; R R Hanson; S A Skinner; R C Rogers; D B Everman; E Boyd; C Tapp; S V Mullegama; D Keelean-Fuller; C M Powell; S H Elsea; C C Morton; J F Gusella; B DuPont; A Chaubey; A E Lin; M E Talkowski
Journal:  Mol Psychiatry       Date:  2013-04-16       Impact factor: 15.992

Review 6.  Epilepsy in Prader-Willi syndrome: clinical, diagnostic and treatment aspects.

Authors:  Alberto Verrotti; Claudia Soldani; Daniela Laino; Renato d'Alonzo; Salvatore Grosso
Journal:  World J Pediatr       Date:  2014-05-07       Impact factor: 2.764

7.  22q and two: 22q11.2 deletion syndrome and coexisting conditions.

Authors:  Jennifer L Cohen; Terrence B Crowley; Daniel E McGinn; Carey McDougall; Marta Unolt; Michele P Lambert; Beverly S Emanuel; Elaine H Zackai; Donna M McDonald-McGinn
Journal:  Am J Med Genet A       Date:  2018-09-23       Impact factor: 2.802

8.  Obesity in adults with 22q11.2 deletion syndrome.

Authors:  Sarah L Voll; Erik Boot; Nancy J Butcher; Samantha Cooper; Tracy Heung; Eva W C Chow; Candice K Silversides; Anne S Bassett
Journal:  Genet Med       Date:  2016-08-18       Impact factor: 8.822

9.  A descriptive study of colorectal function in adults with Prader-Willi Syndrome: high prevalence of constipation.

Authors:  Louise Kuhlmann; Iben Moeller Joensson; Jens Broendum Froekjaer; Klaus Krogh; Stense Farholt
Journal:  BMC Gastroenterol       Date:  2014-04-04       Impact factor: 3.067

10.  Prevalence and risk factors for type 2 diabetes mellitus with Prader-Willi syndrome: a single center experience.

Authors:  Aram Yang; Jinsup Kim; Sung Yoon Cho; Dong-Kyu Jin
Journal:  Orphanet J Rare Dis       Date:  2017-08-30       Impact factor: 4.123

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